Larry Mehrdad, Rabizadeh Soghra, Mohammadi Fatemeh, Yadegar Amirhossein, Jalalpour Azadeh, Mirmiranpour Hossein, Farahmand Ghasem, Esteghamati Alireza, Nakhjavani Manouchehr
Endocrinology and Metabolism Research Center (EMRC), Vali-Asr Hospital Tehran University of Medical Sciences Tehran Iran.
Health Sci Rep. 2024 Sep 29;7(10):e70057. doi: 10.1002/hsr2.70057. eCollection 2024 Oct.
Literature suggests that oxidative stress plays a crucial role in the progression of diabetes. Since poor glycemic control enhances the formation of advanced glycation end-products (AGEs) and advanced oxidation protein products (AOPP) in individuals with diabetes, exploring the association between glycation and oxidative states in diabetes could also shed light on potential consequences. This study evaluated the effects of albuminuria on AGEs and AOPP levels and measured their relationship in participants with type 2 diabetes (T2D) with or without albuminuria.
A cross-sectional, matched case-control study was designed, including 38 T2D subjects with albuminuria and 38 matched T2D subjects with normoalbuminuria. Patients were matched by their body mass index (BMI), age, and duration of diabetes. The unadjusted and adjusted correlation between AGEs and AOPP in the studied groups were analyzed by multiple logistic regression. Using ggplot2, the ties between these two biochemical factors in cases and controls were plotted.
This study elucidated a significant association between AGEs and AOPP in participants with normoalbuminuria ( = 0.331, -value < 0.05), which continued to be significant after controlling for BMI, age, systolic blood pressure (SBP), and diastolic blood pressure (DBP) ( = 0.355, -value < 0.05). However, there was no significant association between AGEs and AOPP in those with albuminuria in the unadjusted model ( = 0.034, -value = 0.841) or after controlling for BMI, age, SBP, and DBP ( = 0.076, -value = 0.685).
Oxidation and glycation molecular biomarkers were correlated in patients without albuminuria; however, this association was not observed in those with albuminuria.
文献表明氧化应激在糖尿病进展中起关键作用。由于血糖控制不佳会增强糖尿病患者体内晚期糖基化终产物(AGEs)和晚期氧化蛋白产物(AOPP)的形成,探索糖尿病中糖化与氧化状态之间的关联也可能揭示潜在后果。本研究评估了蛋白尿对AGEs和AOPP水平的影响,并测量了2型糖尿病(T2D)伴或不伴蛋白尿患者中它们之间的关系。
设计了一项横断面匹配病例对照研究,包括38例有蛋白尿的T2D患者和38例匹配的正常白蛋白尿的T2D患者。患者根据体重指数(BMI)、年龄和糖尿病病程进行匹配。通过多元逻辑回归分析研究组中AGEs和AOPP之间的未调整和调整后的相关性。使用ggplot2绘制病例组和对照组中这两种生化因素之间的关系。
本研究阐明了正常白蛋白尿患者中AGEs和AOPP之间存在显著关联(r = 0.331,P值<0.05),在控制BMI、年龄、收缩压(SBP)和舒张压(DBP)后该关联仍然显著(r = 0.355,P值<0.05)。然而,在未调整模型中,有蛋白尿患者的AGEs和AOPP之间无显著关联(r = 0.034,P值 = 0.841),在控制BMI、年龄、SBP和DBP后也无显著关联(r = 0.076,P值 = 0.685)。
氧化和糖化分子生物标志物在无蛋白尿患者中相关;然而,在有蛋白尿患者中未观察到这种关联。